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审核状态: Project audit state: |
通过审核 Successful |
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注册号: Registration number: |
ChiCTR-IPR-14005475 |
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最近更新日期: Date of Last Refreshed on: |
2016-03-10 18:12:18 |
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注册时间: Date of Registration: |
2014-11-10 00:00:00 |
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注册号状态: |
补注册 |
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Registration Status: |
Retrospective registration |
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注册题目: |
心悦胶囊治疗介入后冠心病的多中心、随机、双盲、安慰剂对照临床研究 |
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Public title: |
Xinyue capsule versus placebo in patients with coronary herat disease after percutaneous coronary intervention: A randomized double-blind placebo-controlled muticenter study |
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注册题目简写: |
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English Acronym: |
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研究课题的正式科学名称: |
心悦胶囊治疗介入后冠心病的多中心、随机、双盲、安慰剂对照临床研究 |
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Scientific title: |
Xinyue capsule versus placebo in patients with coronary herat disease after percutaneous coronary intervention: A randomized double-blind placebo-controlled muticenter study |
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研究课题代号(代码): Study subject ID: |
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在二级注册机构或其它机构的注册号: The registration number of the Partner Registry or other register: |
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申请注册联系人: |
王培利 |
研究负责人: |
史大卓 |
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Applicant: |
Wang Peili |
Study leader: |
Shi Dazhuo |
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申请注册联系人电话: Applicant telephone: |
+86 13691254065 |
研究负责人电话:
Study leader's |
+86 13511072856 |
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申请注册联系人传真 : Applicant Fax: |
研究负责人传真: Study leader's fax: |
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申请注册联系人电子邮件: Applicant E-mail: |
wpl0721@sohu.com |
研究负责人电子邮件: Study leader's E-mail: |
shidazhuo@126.com |
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申请单位网址(自愿提供): Applicant website(voluntary supply): |
研究负责人网址(自愿提供): Study leader's website(voluntary supply): |
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申请注册联系人通讯地址: |
北京市海淀区西苑操场1号 |
研究负责人通讯地址: |
北京市海淀区西苑操场1号 |
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Applicant address: |
1 Xiyuan Chaochang, Haidian district, Beijing |
Study leader's address: |
1 Xiyuan Chaochang, Haidian district, Beijing |
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申请注册联系人邮政编码: Applicant postcode: |
研究负责人邮政编码: Study leader's postcode: |
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申请人所在单位: |
中国中医科学院西苑医院 |
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Applicant's institution: |
Xiyuan Hospital of China Academy of Chinese Medical Sicences |
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研究负责人所在单位: |
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Affiliation of the Leader: |
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是否获伦理委员会批准: |
是 |
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Approved by ethic committee: |
Yes |
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伦理委员会批件文号: Approved No. of ethic committee: |
2013XL059-2 |
伦理委员会批件附件: Approved file of Ethical Committee: |
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批准本研究的伦理委员会名称: |
中国中医科学院西苑医院医学伦理委员会 |
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Name of the ethic committee: |
Medical Ethics Committee of Xiyuan Hospital of China Academy of Chinese Medical Sicences |
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伦理委员会批准日期: Date of approved by ethic committee: |
1990-01-01 00:00:00 | ||
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伦理委员会联系人: |
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Contact Name of the ethic committee: |
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伦理委员会联系地址: |
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Contact Address of the ethic committee: |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
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研究实施负责(组长)单位: |
中国中医科学院西苑医院 |
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Primary sponsor: |
Xiyuan Hospital of China Academy of Chinese Medical Sicences |
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研究实施负责(组长)单位地址: |
北京市海淀区西苑操场1号 |
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Primary sponsor's address: |
1 Xiyuan Caochang, Haidian District, Beijing, China |
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试验主办单位(项目批准或申办者): Secondary sponsor: |
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经费或物资来源: |
吉林省科学技术委员会 |
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Source(s) of funding: |
Science and Technology Committee of Jilin Province |
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研究疾病: |
介入后冠心病 |
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Target disease: |
coronary herat disease after percutaneous coronary intervention |
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研究疾病代码: |
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Target disease code: |
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研究类型: |
干预性研究 |
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Study type: |
Interventional study |
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研究所处阶段: |
上市后药物 | ||||||||||||||||||||||||||||||||||||||||||||
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Study phase: |
4 |
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研究设计: |
随机平行对照 |
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Study design: |
Parallel |
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研究目的: |
通过多中心、随机、双盲、安慰剂对照临床试验,进一步明确心悦胶囊治疗介入治疗后冠心病的疗效和安全性。 |
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Objectives of Study: |
To definite the efficacy and security of xinyue capsule on on coronary herat disease after percutaneous coronary intervention. |
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药物成份或治疗方案详述: |
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Description for medicine or protocol of treatment in detail: |
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纳入标准: |
(1)符合冠心病诊断,并成功行血管介入治疗者; |
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Inclusion criteria |
(1) patients who was suffered coronary heart disease and was accepted sucessful PCI were inclusion; |
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排除标准: |
(1)肾功能不全,男性血清肌酐>2.5 mg/dl(>220umo/l)女性>2.0 mg/dl(>175umo/l); |
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Exclusion criteria: |
(1) concomitant affliction with severe complications including hepatic, renal, and hematopoietic dysfunction, psychiatric disorders, or cancers; |
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研究实施时间: Study execute time: |
从 From 2014-04-01 00:00:00至 To 1990-01-01 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2014-04-01 00:00:00 至 To 1990-01-01 00:00:00 |
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干预措施: Interventions: |
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研究实施地点: Countries of recruitment and research settings: |
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测量指标: Outcomes: |
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采集人体标本:
Collecting sample(s)
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征募研究对象情况: Recruiting status: |
正在进行 Recruiting |
年龄范围: Participant age: |
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性别: |
男女均可 |
Gender: |
Both |
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随机方法(请说明由何人用什么方法产生随机序列): |
由中国中医科学院西苑医院临床药理中心应用SAS统计软件,按参加单位的病例分配数及随机比例生成随机数字分组表。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
An independent, offsite clinical trials statistician at CACMS used a computergenerated randomallocat |
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是否公开试验完成后的统计结果: Calculated Results after the Study Completed public access: |
公开/Public |
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盲法: |
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Blinding: |
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试验完成后的统计结果(上传文件): |
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Calculated Results after
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是否共享原始数据: IPD sharing |
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共享原始数据的方式(说明:请填入公开原始数据日期和方式,如采用网络平台,需填该网络平台名称和网址): |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
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数据采集和管理(说明:数据采集和管理由两部分组成,一为病例记录表(Case Record Form, CRF),二为电子采集和管理系统(Electronic Data Capture, EDC),如ResMan即为一种基于互联网的EDC: |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |